FDA 510(k)

Vivid E80, Vivid E90, Vivid E95

Número K: K220882 · 2022-07-22

RequerenteGe Medical Systems Ultrasound And

Data da decisão2022-07-22

Código do produtoIYN

Comité consultivoRA

DecisãoSubstantially Equivalent

Resumo do dispositivo

Vivid E80, Vivid E90, Vivid E95 is the device name listed in this FDA 510(k) record. The listed applicant is Ge Medical Systems Ultrasound And. It received FDA 510(k) clearance on 2022-07-22 under 510(k) number K220882. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Vivid E80, Vivid E90, Vivid E95?

Vivid E80, Vivid E90, Vivid E95 is a medical device that received FDA 510(k) clearance on 2022-07-22. The listed applicant is Ge Medical Systems Ultrasound And. The 510(k) number is K220882.

When did Vivid E80, Vivid E90, Vivid E95 receive FDA 510(k) clearance?

Vivid E80, Vivid E90, Vivid E95 received FDA 510(k) clearance on 2022-07-22, under 510(k) number K220882.

Who is the listed applicant for Vivid E80, Vivid E90, Vivid E95?

The FDA 510(k) record lists Ge Medical Systems Ultrasound And as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vivid E80, Vivid E90, Vivid E95?

The FDA product code for Vivid E80, Vivid E90, Vivid E95 is IYN.

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Outros registros que listam Ge Medical Systems Ultrasound And como candidato(a)

K200708Vivid iq K200743Vivid E80/ Vivid E90/ Vivid E95 K200138Versana Premier K192917ViewPoint 6

Dispositivos Relacionados (Código: IYN)

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